TY - JOUR
T1 - The Clinicopathologic Characteristics and Genetic Alterations of Gastric Cancer Patients According to the Lauren Classification
AU - Cheng, Han Fang
AU - Huang, Kuo Hung
AU - Chen, Ming Huang
AU - Fang, Wen Liang
AU - Lin, Chien Hsing
AU - Chao, Yee
AU - Lo, Su Shun
AU - Li, Anna Fen Yau
AU - Wu, Chew Wun
AU - Shyr, Yi Ming
N1 - Publisher Copyright:
© 2022 International College of Surgeons. All rights reserved.
PY - 2022
Y1 - 2022
N2 - Objective: The Lauren classification is an important histologic classification of gastric cancer (GC) with different biological behaviors between histologic types. Background: To date, there are few reports on the genetic alterations and survival differences between different histologic types according to the Lauren classification. Methods: In total, 433 GC patients undergoing surgery were enrolled. The clinicopathologic features, prognoses, and genetic alterations of the different Lauren types were compared. Results: Diffuse-type GC was associated with a younger age, female predominance, more Borrmann type 3 and 4 tumors, more advanced pathologic tumor (T) and node (N) categories, more tumor recurrences (especially peritoneal recurrence), and worse 5-year overall survival and disease-free survival rates than intestinal-type GC and mixed-type GC. Regarding genetic alterations, mixed-type GC was associated with more TP53 mutations than intestinal-type GC and diffuse-type GC. Multivariate analysis demonstrated the following independent prognostic factors: age, Lauren classification, and pathologic T and N categories. Regarding mixed-type GC, diffuse-type major tumors were associated with more lymphovascular invasion, a more advanced N category and tumor, node, metastasis stage, and fewer PI3K/AKT pathway mutations than intestinal-type major tumors. Conclusions: Diffuse-type GC had unfavorable clinicopathologic features and a worse prognosis than intestinal-type GC. For mixed-type GC, the clinicopathologic features and genetic alterations were different between intestinal-type major tumors and diffuse-type major tumors.
AB - Objective: The Lauren classification is an important histologic classification of gastric cancer (GC) with different biological behaviors between histologic types. Background: To date, there are few reports on the genetic alterations and survival differences between different histologic types according to the Lauren classification. Methods: In total, 433 GC patients undergoing surgery were enrolled. The clinicopathologic features, prognoses, and genetic alterations of the different Lauren types were compared. Results: Diffuse-type GC was associated with a younger age, female predominance, more Borrmann type 3 and 4 tumors, more advanced pathologic tumor (T) and node (N) categories, more tumor recurrences (especially peritoneal recurrence), and worse 5-year overall survival and disease-free survival rates than intestinal-type GC and mixed-type GC. Regarding genetic alterations, mixed-type GC was associated with more TP53 mutations than intestinal-type GC and diffuse-type GC. Multivariate analysis demonstrated the following independent prognostic factors: age, Lauren classification, and pathologic T and N categories. Regarding mixed-type GC, diffuse-type major tumors were associated with more lymphovascular invasion, a more advanced N category and tumor, node, metastasis stage, and fewer PI3K/AKT pathway mutations than intestinal-type major tumors. Conclusions: Diffuse-type GC had unfavorable clinicopathologic features and a worse prognosis than intestinal-type GC. For mixed-type GC, the clinicopathologic features and genetic alterations were different between intestinal-type major tumors and diffuse-type major tumors.
KW - Clinicopathologic feature
KW - Gastric cancer
KW - Genetic alteration
KW - Lauren classification
KW - Prognosis
UR - http://www.scopus.com/inward/record.url?scp=85130264982&partnerID=8YFLogxK
U2 - 10.9738/INTSURG-D-20-00022.1
DO - 10.9738/INTSURG-D-20-00022.1
M3 - Article
AN - SCOPUS:85130264982
SN - 0020-8868
VL - 106
SP - 39
EP - 47
JO - International Surgery
JF - International Surgery
IS - 1
ER -